EP2011504A1 - Produit dermatologique destiné au traitement et/ou au soin de la peau en cas de neurodermatite - Google Patents

Produit dermatologique destiné au traitement et/ou au soin de la peau en cas de neurodermatite Download PDF

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Publication number
EP2011504A1
EP2011504A1 EP08011814A EP08011814A EP2011504A1 EP 2011504 A1 EP2011504 A1 EP 2011504A1 EP 08011814 A EP08011814 A EP 08011814A EP 08011814 A EP08011814 A EP 08011814A EP 2011504 A1 EP2011504 A1 EP 2011504A1
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EP
European Patent Office
Prior art keywords
composition
silver particles
skin
treatment
atopic dermatitis
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP08011814A
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German (de)
English (en)
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EP2011504B1 (fr
Inventor
Peter Dr. Hansen
Andrea Heppner
Thomas Dr. Rillmann
Christof Schumann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Stada Arzneimittel AG
Original Assignee
Stada Arzneimittel AG
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Publication of EP2011504A1 publication Critical patent/EP2011504A1/fr
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
    • A61K36/18—Magnoliophyta (angiosperms)
    • A61K36/185—Magnoliopsida (dicotyledons)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00—Medicinal preparations containing inorganic active ingredients
    • A61K33/24—Heavy metals; Compounds thereof
    • A61K33/38—Silver; Compounds thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/04—Antipruritics

Definitions

  • the invention relates to the use of silver particles having a mean particle size of 1 to 100 microns for the care of dry skin, especially neurodermitic skin conditions and for the treatment of atopic dermatitis and a composition comprising these silver particles and evening primrose oil and the use of such a composition as a skin care agent, especially in dry skin as well as neurodermitic skin conditions, and for the treatment of atopic dermatitis.
  • Dry skin looks rough, shiny or cracked, sometimes red or flaky. Dry skin can form or increase wrinkles. Dry skin is not just a cosmetic problem, because dry skin can be sensitive, tense and itchy. In addition, dry skin tends to inflammation and may favor the development of eczema.
  • Dry skin can be systemic, often occurs in the elderly, where the epidermis is no longer producing enough lipid, and can be the result of excessive care, dry air, and chronic UV damage.
  • W / O emulsions are usually used, which are to provide the skin with moisture and fat and stabilize the horny layer barrier.
  • Such care agents have no alcohol.
  • Atopic dermatitis is a skin disease whose main symptoms are red, flaky, possibly also weeping eczema on the skin and an often tormenting itching. Other common names for eczema include atopic dermatitis, atopic dermatitis and endogenous eczema. Atopic dermatitis is a chronic inflammatory reaction of the skin.
  • Atopic dermatitis often occurs for the first time in toddlers, but adolescents and adults can also develop eczema for the first time.
  • the symptoms of the disease may be different in different individuals and on different skin areas.
  • the atopic dermatitis can occur in bouts of different duration and strength.
  • atopic dermatitis manifests itself symptomatically, especially in a very sensitive and dry skin, which is often also red.
  • a skin problem is often a strong itching sensation to the affected person. Scratching the skin can cause it to crack, which can lead to eczema, which often wets and aggravates the itching.
  • the most common skin areas affected by atopic dermatitis are the armpits, the popliteal fossae, and the neck and facial areas.
  • cortisone In the prior art many ways of treating atopic dermatitis are known, which in addition to drug therapies and the prevention of certain foods and external stimuli or stress counts.
  • a drug therapy eczema is often treated by cortisone.
  • oral administration of cortisone-containing drugs may also be considered.
  • the disadvantage of cortisone treatment is that it can often only be used for a short time in cases of acute episodes of atopic dermatitis and results in skin thinning, strong hairiness, stretch marks and partial suppression of the local immune system. With prolonged use of cortisone preparations also systemic damage to the organism may occur, such. As liver damage or inducing glaucoma. But other drug therapies, such.
  • This object is achieved by using silver particles of an average particle size of 1 .mu.m to 100 .mu.m in combination with evening primrose oil as dermatics in dry skin, especially neurodermitic skin conditions.
  • silver particles having an average particle size of 1 to 100 ⁇ m are used for the treatment of atopic dermatitis or for the production of a medicament for the treatment of atopic dermatitis.
  • microsilver In the prior art, the antimicrobial action of metallic silver is well known.
  • silver particles of a size of 1 .mu.m to 100 .mu.m so-called microsilver or microsilver are now used for the treatment of atopic dermatitis.
  • silver particles having an average particle size of from 1 ⁇ m to 100 ⁇ m have a positive influence on the symptoms occurring under the clinical picture of atopic dermatitis, such as edema / papule formation, Redness / erythema formation, crusting, excoriation, lichenification, increased itching, dryness (xerosis), scaling and lack of sleep have.
  • Colloidal silver is known in the art. Colloidal silver consists of electrically charged silver particles in water. The particle size of silver in colloidal silver is between 1 and 10 nm. With topical application of this colloidal silver, the silver particles can penetrate into deeper skin layers. The effects of silver nanoparticles on human health when they have invaded the body are not yet known. However, it is known that nanoscale silver, so-called colloidal silver, can deposit in the body at too high a concentration and can lead to so-called silver deposits.
  • the silver particles used according to the invention of a size of 1 ⁇ m to 100 ⁇ m do not have the disadvantages associated with the use of silver nanoparticles of a size of 1 to 100 nm.
  • the silver particles used in the invention are so large that they can not penetrate into the human body when applied topically. They can not be absorbed into the body via the bloodstream.
  • the silver particles according to the present invention have an average particle size of 1 .mu.m to 100 .mu.m, preferably 2 .mu.m to 20 .mu.m and more preferably 2 .mu.m to 5 .mu.m. It is prepared by methods known in the art.
  • the silver particles according to the invention are preferably made of pure silver. But you can also contain in a small proportion of up to 1 wt .-% other metals, such as. As zinc and / or copper. Particularly advantageously, the silver particles impurities of less than 5 ppm, more preferably they are made of pure silver. Possible impurities of the silver particles may, for. As potassium, sodium or chlorine.
  • the silver particles are present in an average particle size of 1 .mu.m to 100 .mu.m as porous particles.
  • the mean inner porosity of the silver particles can be z. B. at least 65%, in particular 65 to 95%. Particularly preferred is an average internal porosity of 85% to 95%.
  • the porosity of the particles can be determined according to the in WO 2005/023213 on page 7.
  • the silver particles used are present as agglomerates of metallic primary particles whose average particle diameter is between 10 and 200 nm, preferably between 15 and 80 nm.
  • Such porous silver particles may according to the in WO 2005/023213 described processes, in particular that on page 10 of WO 2005/023213 described method.
  • Such silver particles having an average particle diameter of 1 .mu.m to 100 .mu.m, which have an inner porosity, are z. B. from the company Biogate available.
  • a combination of the described silver particles having an average particle size of 1 to 100 ⁇ m and evening primrose oil is used for the treatment of atopic dermatitis or for the production of a medicament for the treatment of atopic dermatitis.
  • the treatment of atopic dermatitis both with silver particles of an average particle size of 1 to 100 microns as well as a combination of these silver particles and evening primrose oil can be both a pharmaceutical and a cosmetic and is carried out by topical application of the silver particles, optionally in combination with evening primrose oil to that of atopic dermatitis affected skin.
  • Another object of the present invention are stable compositions comprising the described silver particles having an average particle size of 1 to 100 microns and evening primrose oil.
  • evening primrose oil contains a large amount of unsaturated fatty acids, especially a high proportion of cis-linoleic acid. It is thus very susceptible to spoilage, particularly oxidative spoilage, which is accelerated by the presence of catalytically active metals in compositions containing evening primrose oil.
  • compositions according to the invention has a positive effect in the treatment of dry skin, in particular neurodermitic skin conditions and atopic dermatitis.
  • use of the described silver particles having an average particle size of 1 to 100 .mu.m and evening primrose oil the symptoms of edema / papule formation, reddening / erythema formation, encrustation, excoriation, lichenification, increased itching occurring under the clinical picture of atopic dermatitis , Reduce dryness (xerosis), scaling and lack of sleep or disappear.
  • compositions or remedies according to the invention containing the described silver particles and aftercandy oil are in the form of an O / W emulsion, in particular as an alcoholic O / W emulsion.
  • Dry skin care agents known in the art and agents for the treatment of atopic dermatitis are formulated as a W / O emulsion so that the oil phase is in direct skin contact.
  • the known in the prior art care products for dry skin especially neurodermitic skin conditions, as well as the cure for the treatment of atopic dermatitis alcohol-free, since alcohol dehydrates the skin affected by atopic dermatitis.
  • compositions of the invention which have an O / W galenics, the alcohol contained therein not to another Dehydration of the skin or aggravation of the symptoms occurring at the onset of atopic dermatitis leads, but in addition to the microbiological effect has a pleasant cooling effect and is completely tolerated by the skin.
  • the compositions of the invention are characterized according to a preferred embodiment by an alcohol content of at least 1 wt .-%, in particular 5-15 wt .-% of.
  • compositions according to the invention are characterized in that they are free from PEG emulsifiers, that is to say emulsifiers based on polyethylene glycol, free from preservatives and free from perfumes.
  • compositions according to the invention are formulated as stable silver particle formulations, for example as lotion, paste, ointment, cream, emulsion, gel, powder or suspension.
  • Stable means that the formulation is stable on storage, that is, the silver particles do not sediment during storage and optionally contained evening primrose oil is not decomposed silver-catalytically.
  • the silver particles are present in the compositions according to the invention in amounts of from 0.001% by weight to 10% by weight, preferably from 0.01% by weight to 5% by weight and more preferably from 0.1% by weight Wt .-% and in particular 0.1 wt .-% - 0.5 wt .-% before and are also used according to the claimed use preferably in these ranges.
  • the evening primrose oil is present in the compositions according to the invention in amounts of from 0.1% by weight to 30% by weight, particularly preferably from 1% by weight to 10% by weight, and according to the further claimed use, it is likewise preferred in this composition Quantity range applied.
  • Applicant's study in a study of various compositions comprising silver particles having a mean particle size of 1 to 100 microns and evening primrose oil have a highly significant reduction in the atopic dermatitis associated disorders such as edema / papule formation, redness / erythema formation, crust formation, Excoriation, lichenification, increased itching, dryness (xerosis) and lack of sleep. It has been found that topical application of a composition comprising silver particles having an average particle size of 1 to 100 microns and evening primrose oil lowers the atopy index of atopic dermatitis subjects to topical application of this composition and in many cases even eliminates the neurodermatitis problems.
  • Example 1 Example 2
  • Example 3 Example 4
  • Example 5 Polyglyceryl-3-methylglucose distearate 4.00 4.0 4.2 3.8 4.2 Hydrogenated Coco-Glycerides 1.00 1.00 0.8 1.1 0.8 Cetyl palmitate 1.00 0.9 0.8 1.2 0.9 Cetyl Alcohol 3.00 2.5 2.5 3.2 3 C12-15 alkyl benzoates 8.00 7.8 7.8 8.5 8.2 Simmondsia Chinensis Seed Oil 6.00 5.5 5.5 6 6 isopropyl myristate 5.00 4.5 4.5 5 5 Octyldodecanol, Echium Plantagineum, Cardiospermum, Halicacabum, Helianthus annuus 2.00 1 1 0 0 Evening primrose oil 6.00 4.00 2.00 8.00 5.00 Tocopheryl acetate 1.00 0.8 1.2 1.2 1 MicroSilver 0.30 0.32 0.5 0.25 0.1 Aqua 46,40 53.9 62.14 45.91 55.28 Xanthan gum 0.30 0.28 0.
  • phase I consisting of polyglyceryl-3-methylglucose distearate, hydrogenated coco-glycerides, cetyl palmitate, cetyl alcohol, C12-15 Alkyl Benzoate, Simmondsia Chinensis seed oil, isopropyl myristate, evening primrose oil, tocopheryl acetate and microsilver, and optionally Octyldodecanol, Echium Plantagineum, Cardiospermnum, Halicacabum and Helianthus Annuus, while stirring the heated to 75 ° C phase II, consisting of Aqua, xanthan gum, glycerol and optionally butylene glycol.
  • phase II consisting of Aqua, xanthan gum, glycerol and optionally butylene glycol.
  • the composition is further homogenized, then cooled to 45 ° C and optionally Alcohol Denat added. After further homogenization, the mass is finally cooled with stirring to room temperature.
  • Example 6 Weighing [g / 100g]
  • Example 7 Weighing [g / 100g]
  • Example 8 Weighing [g / 100g]
  • Example 9 Weighing [g / 100g]
  • Example 10 Weighing [g / 100g] Polyglyceryl-3-methylglucose distearate 3.00 3.00 3.2 2.8 2.8 Hydrogenated Coco-Glycerides 0.75 0.75 0.7 0.8 0.8 Cetyl palmitate 0.75 0.75 0.9 0.8 0.7 Cetyl Alcohol 2.25 2.25 2.5 2.2 2.0 C12-15 alkyl benzoates 8.00 8.00 7.8 8.5 8.2 Simmondsia Chinensis Seed Oil 6.00 6.00 4.00 7.00 5.00 isopropyl myristate 5.00 5.00 5.5 5.2 4.8 Octyldodecane, Echium palntagineum, Cardiospernum, Halicacabum, Helianthus, Annus 2.00 2.00 2.5 1 0 Evening primrose oil 6.00 6.00 4.00 2.00 8
  • Table 1 Subjects of the subject collective A number gender Age diagnosis application site 1 w eczema Arms legs 2 w 42 eczema Arms, backs of hands 3 w 50 eczema Arms legs 4 w 44 eczema Arms legs 5 w 47 eczema Arms legs 6 w 18 eczema Arms legs 7 w 44 eczema Forehead, arms 8th w 42 eczema Arms, backs of hands 9 m 43 eczema legs 10 m 40 eczema Arms, backs of hands 11 m 46 eczema poor 12 w 28 eczema poor 13 w 38 eczema Arms, backs of hands 14 w 36 eczema Arms, backs of hands 15 w 66 eczema Arms, backs of hands
  • Subjects of the subject group B number gender Age diagnosis application site 1 w 34 eczema Face, arms and legs 2 w 20 eczema poor 3 w 19 eczema Arms, backs of hands 4 w 45 eczema Arms legs 5 m 34 eczema Arms, backs of hands 6 w 55 eczema poor 7 w 50 eczema Arms legs 8th w 19 eczema Arms legs 9 w 34 eczema Arms legs 10 w 39 eczema Arms, legs, backs of hands 11 w 49 eczema Arms legs 12 w 46 eczema Arms legs 13 m 35 eczema Face, arms, legs 14 w 44 eczema Arms legs 15 w 36 eczema legs
  • the subjects of the groups A and B were given the product cream according to example 1 as well as the subject diaries with the Application instruction given at least twice a day. Furthermore, the subjects were asked to refrain from other preparations in the testarial during the application test.
  • the maximum total value as a modified SCORAD is 50, as an expression of a mean expression of the atopic disease. Calculation of the index: 7A / 2 + B / 5 + C.
  • the evaluation of the subjective assessment criteria was carried out by the subjects as part of the daily documentation in the subject diary.
  • Tables 3-7 summarize the evaluations of the subjective assessment criteria of the subject diaries of the subject collective A, which were prepared after a 10-day application of the cream according to Example 1 in the 18-day period of application of the lotion according to Example 2 from day 11 to day 28.
  • Table 3 gives the subjectively assessed severity of the skin disease.
  • Table 4 shows the subjectively assessed erythema of the skin.
  • Table 5 shows the subjectively assessed dryness of the skin.
  • Table 6 shows the subjectively assessed itching.
  • Table 7 shows the subjectively assessed effect of the investigational medicinal product (here the lotion according to Example 2).
  • Tables 8-12 summarize the evaluations of the subjective assessment criteria of the subject diaries of the subject group B, which was prepared after a 10-day application of the cream according to Example 1 in 18-day period of application of the lotion according to Example 3 from day 11 to day 28.
  • Table 8 gives the subjectively assessed severity of the skin disease.
  • Table 9 shows the subjectively assessed redness.
  • Table 10 shows the subjectively assessed dryness.
  • Table 11 shows the subjectively assessed itching.
  • Table 12 shows the subjectively assessed effect of the investigational medicinal product (here the lotion according to Example 3).
  • Table 13 shows the atopy score of subject group A before application of the lotion of Example 6 on day 11 of the study ("input value”) and after 18 days Application of the lotion according to Example 6 on day 28 of the study ("after 18 days”) and the corresponding absolute and percentage change indicated.
  • the average atopy value decreased from 27.14 to 6.39. This corresponds to a reduction of - 76.44% from baseline.
  • Table 14 shows the atopy score of subject group B before application of the lotion according to Example 7 on day 11 of the study ("input value") and after 18 days application of the lotion according to example 7 on day 28 of the study ("after 18 days”). ) and the corresponding absolute and percentage change.
  • the average atopy value decreased from 19.11 to 6.99. This corresponds to a reduction of - 63.45% from baseline.
  • Table 15 shows the atopy score of subjects A (subjects 1-15) and B (subjects 16-30) before the start of the study ("input value") and at the end of the study, ie after 10 days of application of the cream according to example 1 and 18 daily application of the lotion according to Example 6 in the subject group A or the lotion according to Example 7 in the subject group B reproduced.
  • the index for atopy has decreased values:
  • the atopy score decreases on average by 82.59%.
  • Another object of the present invention is therefore the use of a composition comprising the described silver particles having an average particle size of 1-100 microns and evening primrose oil, in particular present as alcoholic O / W emulsion, for reducing the average atopy score, especially at 18 or 28-day use, by at least 40%, preferably 60%, more preferably 70% and in particular 80%.
  • Table 3 Subject group A, severity of the skin disease, application of lotion according to Example 6 Another 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 No.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
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  • Pharmacology & Pharmacy (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Natural Medicines & Medicinal Plants (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
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  • Biotechnology (AREA)
  • Alternative & Traditional Medicine (AREA)
  • Mycology (AREA)
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  • Inorganic Chemistry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Cosmetics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines Containing Plant Substances (AREA)
EP08011814A 2007-07-06 2008-07-01 Produit dermatologique destiné au traitement et/ou au soin de la peau en cas de neurodermatite Active EP2011504B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102007031650A DE102007031650A1 (de) 2007-07-06 2007-07-06 Dermatikum zur Behandlung und/oder Pflege der Haut bei Neurodermitis

Publications (2)

Publication Number Publication Date
EP2011504A1 true EP2011504A1 (fr) 2009-01-07
EP2011504B1 EP2011504B1 (fr) 2011-12-28

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EP08011814A Active EP2011504B1 (fr) 2007-07-06 2008-07-01 Produit dermatologique destiné au traitement et/ou au soin de la peau en cas de neurodermatite

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Country Link
EP (1) EP2011504B1 (fr)
AT (1) ATE538803T1 (fr)
DE (1) DE102007031650A1 (fr)
ES (1) ES2379474T3 (fr)
PT (1) PT2011504E (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE202011003362U1 (de) 2011-03-01 2011-06-01 Dr. Theiss Naturwaren GmbH, 66424 Zusammensetzung, insbesondere dermatologische Salbe
WO2017093508A1 (fr) * 2015-12-02 2017-06-08 Wild & Natural Ibiza Cosmetics Corp. S.L. Composition pour le soin de la peau
WO2020245569A1 (fr) * 2019-06-06 2020-12-10 Boston Healthcare Limited Composition de traitement de la peau
EP3977858A1 (fr) * 2020-10-01 2022-04-06 Hans Karrer GmbH Crème pour les mains antivirale désinfectante

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030180378A1 (en) 2000-07-27 2003-09-25 Gillis Scott H. Dry powders of metal-containing compounds
WO2005023213A1 (fr) 2003-08-29 2005-03-17 Bio-Gate Ag Produit de soin corporel contenant des particules poreuses d'argent
EP1520577A1 (fr) 2003-09-30 2005-04-06 Kneipp-Werke Kneipp-Mittel-Zentrale GmbH & CO. KG Composition cosmétique ou dermatologique comprenant l'huile d'onagre
DE102004016129A1 (de) 2004-03-31 2005-10-20 Bitop Ag Topische Zubereitung zur Anwendung auf der Haut enthaltend natürliches Öl der Nachtkerze (Oenothera biennis) (=Oleum Oenotherae) und Osmolyte aus extremophilen Mikroorganismen
US20050271743A1 (en) 2001-04-23 2005-12-08 Burrell Robert E Treatment of inflammatory skin conditions
DE102005008299A1 (de) 2005-02-23 2006-12-28 Icb Investment Consulting Beteiligungen Gmbh Universalpflegecreme

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030180378A1 (en) 2000-07-27 2003-09-25 Gillis Scott H. Dry powders of metal-containing compounds
US20050271743A1 (en) 2001-04-23 2005-12-08 Burrell Robert E Treatment of inflammatory skin conditions
WO2005023213A1 (fr) 2003-08-29 2005-03-17 Bio-Gate Ag Produit de soin corporel contenant des particules poreuses d'argent
EP1520577A1 (fr) 2003-09-30 2005-04-06 Kneipp-Werke Kneipp-Mittel-Zentrale GmbH & CO. KG Composition cosmétique ou dermatologique comprenant l'huile d'onagre
DE102004016129A1 (de) 2004-03-31 2005-10-20 Bitop Ag Topische Zubereitung zur Anwendung auf der Haut enthaltend natürliches Öl der Nachtkerze (Oenothera biennis) (=Oleum Oenotherae) und Osmolyte aus extremophilen Mikroorganismen
DE102005008299A1 (de) 2005-02-23 2006-12-28 Icb Investment Consulting Beteiligungen Gmbh Universalpflegecreme

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
HOLTMANN U: "Drug products made from Oenothera biennis oil = Nachtkerzenöl-haltige Produkte. GLS ist nicht gleich GLS", 1 January 1996, TW PAEDIATRIE, KARLSRUHE, DE, PAGE(S) 309,311, ISSN: 0935-3216, XP009107007 *
RING J ET AL: "Evening primrose oil in neurodermatitis? = Nachtkerzenöl bei Neurodermitis?", 1 September 1991, MEDIZINISCHE MONATSSCHRIFT FUER PHARMAZEUTEN, STUTTGART, DE, PAGE(S) 282, ISSN: 0342-9601, XP009107008 *
SWARNA EKANAYAKE-MUDIYANSELAGE ET AL: "Anwendungsbeobachtung mit einem topischen silberhaltigen Pflegeprodukt (Multilind TM MikroSilber Creme) zur Überprüfung der Wirksamkeit, Verträglichkeit und kosmetischen Akzeptanz beim atopischen Ekzem", 1 January 2007, KOSMETISCHE MEDIZIN, GROSSE VERLAG GMBH, BERLIN, DE, PAGE(S) 291 - 295, ISSN: 1430-4031, XP009106957 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE202011003362U1 (de) 2011-03-01 2011-06-01 Dr. Theiss Naturwaren GmbH, 66424 Zusammensetzung, insbesondere dermatologische Salbe
EP2494968A1 (fr) 2011-03-01 2012-09-05 Dr. Theiss Naturwaren GmbH Composition, notamment pommade dermatologique avec de l'huile des fruits d'Olea Europaea et de l'argent
WO2017093508A1 (fr) * 2015-12-02 2017-06-08 Wild & Natural Ibiza Cosmetics Corp. S.L. Composition pour le soin de la peau
WO2020245569A1 (fr) * 2019-06-06 2020-12-10 Boston Healthcare Limited Composition de traitement de la peau
EP3977858A1 (fr) * 2020-10-01 2022-04-06 Hans Karrer GmbH Crème pour les mains antivirale désinfectante

Also Published As

Publication number Publication date
ES2379474T3 (es) 2012-04-26
EP2011504B1 (fr) 2011-12-28
ATE538803T1 (de) 2012-01-15
PT2011504E (pt) 2012-04-10
DE102007031650A1 (de) 2009-01-08

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